JP2019131637A - Lubricant composition, manufacturing method of lubricant composition and non-stage transmission - Google Patents
Lubricant composition, manufacturing method of lubricant composition and non-stage transmission Download PDFInfo
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/02—Well-defined hydrocarbons
- C10M105/04—Well-defined hydrocarbons aliphatic
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/38—Esters of polyhydroxy compounds
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- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/02—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a non-macromolecular organic compound
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16H—GEARING
- F16H15/00—Gearings for conveying rotary motion with variable gear ratio, or for reversing rotary motion, by friction between rotary members
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/04—Well-defined cycloaliphatic compounds
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/04—Well-defined cycloaliphatic compounds
- C10M2203/045—Well-defined cycloaliphatic compounds used as base material
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
- C10M2203/065—Well-defined aromatic compounds used as base material
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/2805—Esters used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
- C10M2207/2815—Esters of (cyclo)aliphatic monocarboxylic acids used as base material
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
- C10M2207/2835—Esters of polyhydroxy compounds used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/071—Branched chain compounds
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/02—Pour-point; Viscosity index
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/74—Noack Volatility
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/045—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for continuous variable transmission [CVT]
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Abstract
Description
本発明は、潤滑油組成物、潤滑油組成物の製造方法及び無段変速機に関する。 The present invention relates to a lubricating oil composition, a method for producing a lubricating oil composition, and a continuously variable transmission.
無段変速機、とりわけトラクションドライブ方式の変速機は、歯車を用いた変速機と比べて小型かつ軽量であり、金属間の接触を伴わずに変速できることから、ノイズが発生しにくいという特徴を有している。そのため、トラクションドライブ方式の変速機は、特に電気自動車を中心に、その適用が検討されるようになっている。 Continuously variable transmissions, especially traction drive type transmissions, are smaller and lighter than gear-type transmissions, and can change gears without contact between metals, making them less susceptible to noise. doing. For this reason, application of traction drive type transmissions is being studied, particularly for electric vehicles.
トラクションドライブ方式の変速機に用いられる潤滑油組成物には、大きいトルク伝達容量を確保する観点から高温条件下(例えば、自動車用途であれば120℃程度)における高トラクション係数とともに、例えば北米、北欧といった寒冷地における低温始動性を確保するために、低温条件下(例えば、−40℃程度)でも粘度が低いという低温流動性が求められるが、これらの性能は相反する性能であるため、その両立は難しい。このような性能を有する潤滑油組成物として、所定の引火点を有するナフテン系合成潤滑油基油とパラフィン系合成潤滑油基油とを所定含有量で含む潤滑油基油組成物、更にはポリα−オレフィンを含む潤滑油基油組成物が提案されている(例えば、特許文献1)。 Lubricating oil compositions used in traction drive transmissions include, for example, North America and Northern Europe, together with a high traction coefficient under high temperature conditions (for example, about 120 ° C. for automobile applications) from the viewpoint of securing a large torque transmission capacity. In order to ensure low temperature startability in cold regions, low temperature fluidity is required such that the viscosity is low even under low temperature conditions (for example, about −40 ° C.). Is difficult. As a lubricating oil composition having such a performance, a lubricating base oil composition comprising a predetermined content of a naphthenic synthetic lubricating base oil and a paraffinic synthetic lubricating base oil having a predetermined flash point, A lubricating base oil composition containing an α-olefin has been proposed (for example, Patent Document 1).
ところで近年、特に自動車用の無段変速機、中でもトラクションドライブ方式の変速機に用いられる潤滑油組成物に対する高トラクション係数、低温流動性等の要求性能は益々厳しくなっており、上記の潤滑油基油組成物では対応できない場合が増えている。また、高トラクション係数、低温流動性等の性能に加えて、取扱安全性の観点から高い引火点、例えば140℃以上の引火点も求められるようになっている。 In recent years, the required performance such as high traction coefficient and low-temperature fluidity for lubricating oil compositions used for continuously variable transmissions for automobiles, in particular, traction drive type transmissions, has become increasingly severe. The number of cases where the oil composition cannot cope is increasing. Further, in addition to performance such as a high traction coefficient and low temperature fluidity, a high flash point, for example, a flash point of 140 ° C. or higher, is required from the viewpoint of handling safety.
本発明は、上記事情に鑑みてなされたものであり、高トラクション係数と優れた低温流動性とをより高い次元で両立するとともに、高引火点を有する潤滑油組成物、該潤滑油組成物の製造方法、及び該潤滑油組成物を用いた無段変速機を提供することを目的とする。 The present invention has been made in view of the above circumstances, and has a high traction coefficient and excellent low-temperature fluidity at a higher level, and a lubricating oil composition having a high flash point. It is an object of the present invention to provide a manufacturing method and a continuously variable transmission using the lubricating oil composition.
本発明者は、上記課題に鑑みて鋭意検討の結果、所定のナフテン系合成油とエステルとを、所定の含有量で組み合わせた潤滑油組成物、すなわち、引火点が140℃以上のナフテン系合成油(a)及び分岐鎖を有する炭素数5〜32のエステル(b)を含み、該ナフテン系合成油(a)の組成物全量基準の含有量が35質量%以上80質量%未満である潤滑油組成物により、上記課題を解決できることを見出した。 As a result of intensive studies in view of the above problems, the inventor has obtained a lubricating oil composition in which a predetermined naphthenic synthetic oil and an ester are combined at a predetermined content, that is, a naphthenic synthetic having a flash point of 140 ° C. or higher. Lubricant comprising an oil (a) and a C5-C32 ester (b) having a branched chain, and the content of the naphthenic synthetic oil (a) based on the total composition is 35% by mass or more and less than 80% by mass It discovered that the said subject could be solved with an oil composition.
本発明によれば、高トラクション係数と優れた低温流動性とをより高い次元で両立するとともに、高引火点を有する潤滑油組成物、該潤滑油組成物の製造方法、及び該潤滑油組成物を用いた無段変速機を提供することができる。 According to the present invention, a high traction coefficient and excellent low temperature fluidity can be achieved at a higher level, and a lubricating oil composition having a high flash point, a method for producing the lubricating oil composition, and the lubricating oil composition A continuously variable transmission using the can be provided.
以下、本発明の実施形態(以後、単に「本実施形態」と称する場合がある。)について説明する。なお、本明細書中において、数値範囲の記載に関する「以上」、「以下」及び「〜」に係る数値は任意に組み合わせできる数値である。 Hereinafter, an embodiment of the present invention (hereinafter simply referred to as “this embodiment”) will be described. In addition, in this specification, the numerical value concerning "above", "below", and "-" regarding description of a numerical range is a numerical value which can be combined arbitrarily.
[潤滑油組成物]
本実施形態の潤滑油組成物は、引火点が140℃以上のナフテン系合成油(a)及び分岐鎖を有する炭素数5〜32のエステル(b)を含み、該ナフテン系合成油(a)の組成物全量基準の含有量が35質量%以上80質量%未満、というものである。以下、本実施形態の潤滑油組成物が含有し得る各成分について具体的に説明する。
[Lubricating oil composition]
The lubricating oil composition of the present embodiment includes a naphthenic synthetic oil (a) having a flash point of 140 ° C. or more and a C5-C32 ester (b) having a branched chain, and the naphthenic synthetic oil (a). The content based on the total amount of the composition is 35% by mass or more and less than 80% by mass. Hereinafter, each component which the lubricating oil composition of this embodiment may contain is demonstrated concretely.
(ナフテン系合成油(a))
本実施形態の潤滑油組成物は、引火点が140℃以上のナフテン系合成油(a)(以下、「ナフテン系合成油(a)」と称することがある。)の組成物全量基準の含有量が35質量%以上80質量%未満であることを要する。本実施形態の潤滑油組成物において、ナフテン系合成油(a)の組成物全量基準の含有量が35質量%以上80質量%未満でないと、高トラクション係数と優れた低温流動性とをより高い次元で両立することができず、高引火点が得られなくなる。
(Naphthenic synthetic oil (a))
The lubricating oil composition of the present embodiment contains a naphthenic synthetic oil (a) having a flash point of 140 ° C. or higher (hereinafter sometimes referred to as “naphthenic synthetic oil (a)”) based on the total amount of the composition. The amount is required to be 35% by mass or more and less than 80% by mass. In the lubricating oil composition of the present embodiment, if the content of the naphthenic synthetic oil (a) based on the total composition is not 35% by mass or more and less than 80% by mass, the high traction coefficient and the excellent low-temperature fluidity are higher. It is impossible to achieve a balance between dimensions, and a high flash point cannot be obtained.
本実施形態の潤滑油組成物において、ナフテン系合成油(a)の引火点は140℃以上であることを要する。引火点が140℃未満のものであると、特に高トラクション係数が得られず、また高引火点の潤滑油組成物が得られなくなる。トラクション係数、及び引火点を向上させる観点から、ナフテン系合成油(a)の引火点は、好ましくは145℃以上、より好ましくは150℃以上、更に好ましくは160℃以上であり、上限は特に制限はないが、200℃以下程度であればよい。なお、本明細書において、引火点は、JIS K2265−4:2007(引火点の求め方−第4部:クリーブランド開放法)に準拠し、クリーブランド開放法により測定される引火点である。 In the lubricating oil composition of the present embodiment, the flash point of the naphthenic synthetic oil (a) needs to be 140 ° C. or higher. When the flash point is less than 140 ° C., a particularly high traction coefficient cannot be obtained, and a lubricating oil composition having a high flash point cannot be obtained. From the viewpoint of improving the traction coefficient and the flash point, the flash point of the naphthenic synthetic oil (a) is preferably 145 ° C. or higher, more preferably 150 ° C. or higher, further preferably 160 ° C. or higher, and the upper limit is particularly limited. However, it may be about 200 ° C. or less. In addition, in this specification, a flash point is a flash point measured by the Cleveland open method in accordance with JIS K2265-4: 2007 (How to find a flash point-Part 4: Cleveland open method).
本実施形態の潤滑油組成物において用いられるナフテン系合成油(a)としては、引火点が140℃以上であれば特に制限はないが、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、環状構造部分を有しているものが好ましく、より好ましくはシクロヘキサン環、ビシクロヘプタン環及びビシクロオクタン環から選ばれる少なくとも一種の環を有する合成油であることが好ましい。このようなナフテン系合成油(a)としては、例えば、下記一般式(1)で表される合成油が挙げられる。 The naphthenic synthetic oil (a) used in the lubricating oil composition of the present embodiment is not particularly limited as long as the flash point is 140 ° C. or higher, but has a higher traction coefficient and excellent low temperature fluidity. From the viewpoint of improving the flash point, it is preferable to have a cyclic structure portion, more preferably a synthetic oil having at least one ring selected from a cyclohexane ring, a bicycloheptane ring and a bicyclooctane ring. Preferably there is. Examples of such naphthenic synthetic oil (a) include synthetic oils represented by the following general formula (1).
一般式(1)中、R11及びR13はそれぞれ独立に1価の炭化水素基を示し、R12は2価の炭化水素基を示し、X11及びX12はそれぞれ独立にシクロへキサン環、ビシクロヘプタン環又はビシクロオクタン環を示し、p11及びp12はそれぞれ独立に1以上6以下の整数を示す。 In general formula (1), R 11 and R 13 each independently represent a monovalent hydrocarbon group, R 12 represents a divalent hydrocarbon group, and X 11 and X 12 each independently represent a cyclohexane ring. , Bicycloheptane ring or bicyclooctane ring, p 11 and p 12 each independently represents an integer of 1 or more and 6 or less.
R11及びR13の1価の炭化水素基としては、例えばアルキル基、アルケニル基、アルカジエン基、シクロアルキル基、アリール基等が挙げられる。高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、これらの1価の炭化水素基の中でも、アルキル基、アルケニル基が好ましく、アルキル基がより好ましい。また、これらの1価の炭化水素基は直鎖状、分岐状、環状のいずれであってもよく、ハロゲン原子、水酸基、1価の炭化水素基がシクロアルキル基、アリール基の場合は更にアルキル基等の置換基を有していてもよい。
また、これと同様の観点から、1価の炭化水素基の炭素数としては、1価の炭化水素基がアルキル基の場合、好ましくは1以上であり、上限として好ましくは12以下、より好ましくは8以下、更に好ましくは4以下であり、特に好ましくは2以下であり、1価の炭化水素がアルケニル基の場合、2以上であり、好ましくは3以上、上限として好ましくは12以下、より好ましくは8以下、更に好ましくは4以下である。
Examples of the monovalent hydrocarbon group for R 11 and R 13 include an alkyl group, an alkenyl group, an alkadiene group, a cycloalkyl group, and an aryl group. Of these monovalent hydrocarbon groups, an alkyl group and an alkenyl group are preferable, and an alkyl group is more preferable from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. preferable. These monovalent hydrocarbon groups may be linear, branched or cyclic. When the halogen atom, hydroxyl group or monovalent hydrocarbon group is a cycloalkyl group or an aryl group, an alkyl group is further added. It may have a substituent such as a group.
Further, from the same viewpoint, the carbon number of the monovalent hydrocarbon group is preferably 1 or more when the monovalent hydrocarbon group is an alkyl group, and the upper limit is preferably 12 or less, more preferably 8 or less, more preferably 4 or less, particularly preferably 2 or less, and when the monovalent hydrocarbon is an alkenyl group, it is 2 or more, preferably 3 or more, and the upper limit is preferably 12 or less, more preferably 8 or less, more preferably 4 or less.
p11及びp12はそれぞれ独立に1以上6以下の整数であり、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、上限として好ましくは4以下、より好ましくは3以下、更に好ましくは2以下である。 p 11 and p 12 are each independently an integer of 1 or more and 6 or less, and preferably 4 as the upper limit from the viewpoint of achieving both a high traction coefficient and excellent low temperature fluidity at a higher level and improving the flash point. Below, more preferably 3 or less, and still more preferably 2 or less.
R12の2価の炭化水素基としては、上記R11及びR13の1価の炭化水素基より一つの水素原子を除去して2価となったものが挙げられ、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、好ましくはアルキレン基、アルケニレン基、より好ましくはアルキレン基である。
また、これと同様の観点から、R12の2価の炭化水素基の炭素数は、1以上であり、上限として好ましくは12以下、より好ましくは8以下、更に好ましくは4以下である。
Examples of the divalent hydrocarbon group of R 12 include those obtained by removing one hydrogen atom from the monovalent hydrocarbon group of R 11 and R 13 to be divalent, and have a high traction coefficient and excellent performance. From the viewpoints of achieving both low temperature fluidity at a higher level and improving the flash point, an alkylene group, an alkenylene group, and more preferably an alkylene group.
Further, from the same viewpoint, the carbon number of the divalent hydrocarbon group of R 12 is 1 or more, and the upper limit is preferably 12 or less, more preferably 8 or less, and still more preferably 4 or less.
X11及びX12の環としては、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、ビシクロヘプタン環、ビシクロオクタン環が好ましく、ビシクロヘプタン環がより好ましい。
ビシクロヘプタン環としては、例えばビシクロ[2.2.1]ヘプタン環、ビシクロ[3.3.0]ヘプタン環が挙げられ、ビシクロオクタン環としては、例えば、ビシクロ[3.2.1]オクタン環、ビシクロ[2.2.2]オクタン環が挙げられる。これらの中でも、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、ビシクロ[2.2.1]ヘプタン環、ビシクロ[3.3.0]ヘプタン環が好ましく、特にビシクロ[2.2.1]ヘプタン環が好ましい。
また、これらの環は上記R11及びR13の1価の炭化水素基を有するほか、その他、例えば水酸基、ハロゲン原子等の置換基を有してもよい。
As the ring of X 11 and X 12 , a bicycloheptane ring and a bicyclooctane ring are preferable from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. Is more preferable.
Examples of the bicycloheptane ring include a bicyclo [2.2.1] heptane ring and a bicyclo [3.3.0] heptane ring. Examples of the bicyclooctane ring include a bicyclo [3.2.1] octane ring. And bicyclo [2.2.2] octane ring. Among these, from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point, a bicyclo [2.2.1] heptane ring and a bicyclo [3.3.0] A heptane ring is preferable, and a bicyclo [2.2.1] heptane ring is particularly preferable.
In addition to the monovalent hydrocarbon groups of R 11 and R 13 , these rings may have a substituent such as a hydroxyl group or a halogen atom.
本実施形態において、上記の中でも、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、R11及びR13がそれぞれ独立にアルキル基又はアルケニル基であり、R12がアルキレン基又はアルケニレン基である組み合わせが好ましく、R11及びR13がそれぞれ独立に炭素数1以上4以下のアルキル基であり、R12が炭素数1以上4以下のアルキレン基であり、p11及びp12がそれぞれ独立に1又は2である組み合わせがより好ましく、R11及びR13がそれぞれ独立に炭素数1以上4以下のアルキル基であり、R12が炭素数1以上4以下のアルキレン基であり、X11及びX12がビシクロヘプタン環であり、p11及びp12がそれぞれ独立に1又は2である組み合わせが更に好ましく、R11及びR13がそれぞれ独立に炭素数1以上2以下のアルキル基であり、R12が炭素数1以上2以下のアルキレン基であり、X11及びX12がビシクロ[2.2.1]ヘプタン環であり、p11及びp12がそれぞれ独立に1又は2である組み合わせが特に好ましい。 In the present embodiment, among the above, R 11 and R 13 are each independently an alkyl group or an alkenyl group from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. And a combination in which R 12 is an alkylene group or an alkenylene group is preferred, R 11 and R 13 are each independently an alkyl group having 1 to 4 carbon atoms, and R 12 is an alkylene group having 1 to 4 carbon atoms. And a combination in which p 11 and p 12 are each independently 1 or 2 is more preferable, R 11 and R 13 are each independently an alkyl group having 1 to 4 carbon atoms, and R 12 is 1 or more carbon atoms. 4 is a less alkylene group, X 11 and X 12 are bicycloheptane ring, p 11 and p 12 are each independently 1 or 2 More preferably a combination that, R 11 and R 13 are each independently an alkyl group having 1 to 2 carbon atoms, R 12 is an alkylene group having 1 to 2 carbon atoms, X 11 and X 12 is bicyclo [ 2.2.1] A heptane ring in which p 11 and p 12 are each independently 1 or 2 is particularly preferred.
ナフテン系合成油(a)の組成物全量基準の含有量は、35質量%以上80質量%未満であることを要する。ナフテン系合成油(a)の含有量が35質量%未満であると、高トラクション係数が得られず、また高引火点も得られない。一方、ナフテン系合成油(a)の含有量が80質量%以上であると、優れた低温流動性が得られなくなる。
ナフテン系合成油(a)の組成物全量基準の含有量は、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、好ましくは40質量%以上、より好ましくは45質量%以上、更に好ましくは50質量%以上、特に好ましくは60質量%以上であり、上限として好ましくは79質量%以下、より好ましくは77質量%以下、更に好ましくは75質量%以下である。また、本実施形態において、上記ナフテン系合成油(a)は単独で、又は複数種を組み合わせて用いてもよく、複数種を組み合わせて用いる場合は、該複数種のナフテン系合成油(a)の合計含有量が上記含有量の範囲内となっていればよい。
The content of the naphthenic synthetic oil (a) based on the total composition amount is required to be 35% by mass or more and less than 80% by mass. When the content of the naphthenic synthetic oil (a) is less than 35% by mass, a high traction coefficient cannot be obtained, and a high flash point cannot be obtained. On the other hand, when the content of the naphthenic synthetic oil (a) is 80% by mass or more, excellent low temperature fluidity cannot be obtained.
The content based on the total amount of the composition of the naphthenic synthetic oil (a) is preferably 40% by mass or more from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. More preferably, it is 45% by mass or more, more preferably 50% by mass or more, particularly preferably 60% by mass or more, and the upper limit is preferably 79% by mass or less, more preferably 77% by mass or less, still more preferably 75% by mass. It is as follows. In the present embodiment, the naphthenic synthetic oil (a) may be used singly or in combination of a plurality of types, and when used in combination of a plurality of types, the plurality of naphthenic synthetic oils (a). It is sufficient that the total content of is within the range of the above content.
(分岐鎖を有する炭素数5〜32のエステル(b))
本実施形態の潤滑油組成物は、分岐鎖を有する炭素数5〜32のエステル(b)(以下、「エステル(b)」と称することがある。)を含む。本実施形態の潤滑油組成物において、エステル(b)を含まないと、特に低温流動性が得られない。
(Branched C5-C32 Ester (b))
The lubricating oil composition of the present embodiment contains an ester (b) having a branched chain and having 5 to 32 carbon atoms (hereinafter sometimes referred to as “ester (b)”). If the lubricating oil composition of this embodiment does not contain the ester (b), particularly low temperature fluidity cannot be obtained.
エステル(b)としては、分岐鎖を有し、炭素数5〜32であり、かつエステル構造を有するものであれば特に制限はないが、好ましくは下記一般式(2)で表されるモノエステル、下記一般式(3)で表されるジエステルが挙げられる。 The ester (b) is not particularly limited as long as it has a branched chain, has 5 to 32 carbon atoms, and has an ester structure, but is preferably a monoester represented by the following general formula (2) And diesters represented by the following general formula (3).
一般式(2)中、R21及びR22は、それぞれ独立に炭素数3以上の分岐状の1価の炭化水素基を示す。また、一般式(3)中、R31及びR32は、それぞれ独立に炭素数3以上の分岐状の1価の炭化水素基を示し、X31は炭素数3以上の分岐状の2価の炭化水素基を示す。 In the general formula (2), R 21 and R 22 each independently represent a branched monovalent hydrocarbon group having 3 or more carbon atoms. In the general formula (3), R 31 and R 32 each independently represent a branched monovalent hydrocarbon group having 3 or more carbon atoms, and X 31 represents a branched divalent hydrocarbon group having 3 or more carbon atoms. A hydrocarbon group is shown.
一般式(2)において、R21及びR22の炭素数3以上の分岐状の1価の炭化水素基としては、上記R11及びR13の1価の炭化水素基として例示した基のうち、炭素数3以上であり、かつ分岐状である基が挙げられる。中でも、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、分岐状のアルキル基、アルケニル基が好ましく、アルキル基がより好ましい。また炭素数としては、好ましくは4以上、より好ましくは5以上、更に好ましくは6以上であり、上限として好ましくは16以下、より好ましくは14以下、更に好ましくは12以下である。 In the general formula (2), as the branched monovalent hydrocarbon group having 3 or more carbon atoms of R 21 and R 22 , among the groups exemplified as the monovalent hydrocarbon group of R 11 and R 13 above, Examples thereof include a group having 3 or more carbon atoms and a branched shape. Of these, branched alkyl groups and alkenyl groups are preferred, and alkyl groups are more preferred from the viewpoints of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. The number of carbon atoms is preferably 4 or more, more preferably 5 or more, and further preferably 6 or more, and the upper limit is preferably 16 or less, more preferably 14 or less, and still more preferably 12 or less.
また、R21及びR22の1価の炭化水素基は、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、gem−ジアルキル構造を有する分岐状の基であることが好ましい。この場合、gem−ジアルキル構造におけるアルキル基の炭素数は、好ましくは1以上であり、上限として好ましくは4以下、より好ましくは3以下、更に好ましくは2以下であり、2つのアルキル基の炭素数は同じでも異なっていてもよい。特に好ましいgem−ジアルキル構造は、該構造におけるアルキル基の炭素数がいずれも1である、gem−ジメチル構造である。
このようなR21及びR22の1価の炭化水素基の典型的な例としては、イソプロピル基、1,1−ジメチルエチル基、2,2−ジメチルプロピル基、3,3−ジメチルブチル基、4,4−ジメチルペンチル基、5,5−ジメチルヘキシル基、2,4,4−トリメチルペンチル基、3,5,5−トリメチルへキシル基、2,2,4,4,6−ペンタメチルヘプチル基、2,2,4,6,6−ペンタメチルヘプチル基、3,5,5,7,7−ペンタメチルオクチル基等が好ましく挙げられる。なお、これらの1価の炭化水素基はあくまで典型的なものを例示するものであり、本実施形態においては、上記例示の炭化水素基の異性体をR21及びR22として有するものであってもよいことは言うまでもない。
Moreover, the monovalent hydrocarbon group of R 21 and R 22 is a branch having a gem-dialkyl structure from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. It is preferably a group having a shape. In this case, the carbon number of the alkyl group in the gem-dialkyl structure is preferably 1 or more, and the upper limit is preferably 4 or less, more preferably 3 or less, still more preferably 2 or less, and the carbon number of the two alkyl groups. May be the same or different. A particularly preferred gem-dialkyl structure is a gem-dimethyl structure in which all of the alkyl groups in the structure have 1 carbon.
Typical examples of such monovalent hydrocarbon groups for R 21 and R 22 include isopropyl group, 1,1-dimethylethyl group, 2,2-dimethylpropyl group, 3,3-dimethylbutyl group, 4,4-dimethylpentyl group, 5,5-dimethylhexyl group, 2,4,4-trimethylpentyl group, 3,5,5-trimethylhexyl group, 2,2,4,4,6-pentamethylheptyl Preferred examples include a group, 2,2,4,6,6-pentamethylheptyl group, 3,5,5,7,7-pentamethyloctyl group and the like. These monovalent hydrocarbon groups are merely exemplary, and in the present embodiment, the above-exemplified hydrocarbon group isomers are represented as R 21 and R 22. Needless to say.
エステル(b)がモノエステルの場合、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、炭素数は好ましくは8以上、より好ましくは12以上、更に好ましくは16以上であり、上限として好ましくは30以下、より好ましくは25以下、更に好ましくは21以下である。 When the ester (b) is a monoester, the carbon number is preferably 8 or more, more preferably 12 or more, from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. More preferably, it is 16 or more, and the upper limit is preferably 30 or less, more preferably 25 or less, and still more preferably 21 or less.
一般式(3)において、R31及びR32の炭素数3以上の分岐状の1価の炭化水素基としては、R21及びR22の炭素数3以上の分岐状の1価の炭化水素基と同じものが挙げられる。中でも、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、分岐状のアルキル基、アルケニル基が好ましく、アルキル基がより好ましい。また炭素数の上限として好ましくは16以下、より好ましくは14以下、更に好ましくは10以下である。 In the general formula (3), the branched monovalent hydrocarbon group having 3 or more carbon atoms of R 31 and R 32 is a branched monovalent hydrocarbon group having 3 or more carbon atoms of R 21 and R 22. The same thing is mentioned. Of these, branched alkyl groups and alkenyl groups are preferred, and alkyl groups are more preferred from the viewpoints of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. The upper limit of the carbon number is preferably 16 or less, more preferably 14 or less, and still more preferably 10 or less.
X31の2価の炭化水素基としては、上記R31及びR32の1価の炭化水素基より一つの水素原子を除去して2価となったものが挙げられ、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、好ましくはアルキレン基、アルケニレン基、より好ましくはアルキレン基であり、上記R21及びR22と同じく、gem−ジアルキル構造を有していることが好ましい。
これと同様の観点から、X31の2価の炭化水素基の炭素数は、好ましくは4以上、より好ましくは5以上、更に好ましくは6以上であり、上限として好ましくは16以下、より好ましくは14以下、更に好ましくは12以下である。
Examples of the divalent hydrocarbon group of X 31 include those obtained by removing one hydrogen atom from the monovalent hydrocarbon group of R 31 and R 32 to be divalent, and have a high traction coefficient and excellent performance. From the viewpoint of achieving both low temperature fluidity at a higher level and improving the flash point, it is preferably an alkylene group, an alkenylene group, more preferably an alkylene group, and the gem-dialkyl structure as in R 21 and R 22 above. It is preferable to have.
From the same viewpoint, the carbon number of the divalent hydrocarbon group of X 31 is preferably 4 or more, more preferably 5 or more, still more preferably 6 or more, and the upper limit is preferably 16 or less, more preferably 14 or less, more preferably 12 or less.
エステル(b)がジエステルの場合、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、炭素数は好ましくは11以上、より好ましくは12以上、更に好ましくは14以上であり、上限として好ましくは30以下、より好ましくは28以下、更に好ましくは26以下である。 When the ester (b) is a diester, the carbon number is preferably 11 or more, more preferably 12 or more, from the viewpoint of achieving both a high traction coefficient and excellent low-temperature fluidity at a higher level and improving the flash point. More preferably, it is 14 or more, and the upper limit is preferably 30 or less, more preferably 28 or less, and still more preferably 26 or less.
本実施形態において、一般式(3)で表されるジエステルとしては、上記の中でも、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させる観点から、R31及びR32がそれぞれ独立に炭素数3以上16以下の分岐状のアルキル基又はアルケニル基であり、X31が炭素数3以上16以下の分岐状のアルキレン基又はアルケニレン基である組み合わせが好ましく、R31及びR32がそれぞれ独立に炭素数3以上16以下の分岐状のアルキル基であり、X31が炭素数3以上16以下の分岐状のアルキレン基である組み合わせがより好ましく、R31及びR32がそれぞれ独立にgem−ジアルキル構造を有する炭素数3以上16以下の分岐状のアルキル基であり、X31が炭素数3以上16以下の分岐状のアルキレン基である組み合わせが更に好ましい。 In the present embodiment, as the diester represented by the general formula (3), among the above, from the viewpoint of achieving both a high traction coefficient and excellent low temperature fluidity at a higher level and improving the flash point, R 31 and R 32 are each independently a branched alkyl group or alkenyl group having 3 to 16 carbon atoms, and a combination in which X 31 is a branched alkylene group or alkenylene group having 3 to 16 carbon atoms is preferable, R 31 and R 32 are each independently an alkyl group having 3 to 16 branched carbon, more preferably the combination X 31 is an alkylene group branched having 3 to 16 carbon atoms, R 31 and R 32 is a branched alkyl group having 3 to 16 carbon atoms having independently gem- dialkyl structure, X 31 is 3 or more carbon atoms 16 More preferably a combination a branched alkylene group below.
エステル(b)の組成物全量基準の含有量は、好ましくは10質量%以上、より好ましくは12質量%以上、更に好ましくは15質量%以上、特に好ましくは20質量%以上であり、上限として好ましくは65質量%以下、より好ましくは60質量%以下、更に好ましくは55質量%以下、特に好ましくは50質量%以下である。エステル(b)の含有量が上記範囲内であると、高トラクション係数と優れた低温流動性とをより高い次元で両立させ、かつ引火点を向上させることができ、特に優れた低温流動性の向上効果が得られる。また、本実施形態において、上記エステル(b)は単独で、又は複数種を組み合わせて用いてもよく、複数種を組み合わせて用いる場合は、該複数種のエステル(b)の合計含有量が上記含有量の範囲内となっていればよい。 The content of the ester (b) based on the total amount of the composition is preferably 10% by mass or more, more preferably 12% by mass or more, still more preferably 15% by mass or more, and particularly preferably 20% by mass or more. Is 65% by mass or less, more preferably 60% by mass or less, still more preferably 55% by mass or less, and particularly preferably 50% by mass or less. When the content of the ester (b) is within the above range, a high traction coefficient and excellent low temperature fluidity can be achieved at a higher level and the flash point can be improved. Improvement effect is obtained. Moreover, in this embodiment, the said ester (b) may be used individually or in combination of multiple types, and when using it in combination of multiple types, the total content of the multiple types of esters (b) is the above. It may be within the range of the content.
(その他添加剤)
本実施形態の潤滑油組成物は、上記ナフテン系合成油(a)及びエステル(b)を含むものであり、ナフテン系合成油(a)及びエステル(b)からなるものであってもよいし、また、ナフテン系合成油(a)及びエステル(b)以外に、例えば、粘度指数向上剤、分散剤、酸化防止剤、極圧剤、金属不活性化剤、消泡剤等のその他添加剤を含むものであってもよい。これらのその他添加剤は、単独で、又は複数種を組み合わせて用いることができる。
これらのその他添加剤の合計含有量は、所望に応じて適宜決定すればよく、特に制限はないが、その他添加剤を添加する効果を考慮すると、組成物全量基準で、0.1〜20質量%が好ましく、1〜15質量%がより好ましく、5〜13質量%が更に好ましい。
(Other additives)
The lubricating oil composition of the present embodiment contains the naphthenic synthetic oil (a) and the ester (b), and may consist of the naphthenic synthetic oil (a) and the ester (b). In addition to naphthenic synthetic oil (a) and ester (b), other additives such as viscosity index improvers, dispersants, antioxidants, extreme pressure agents, metal deactivators, antifoaming agents, etc. May be included. These other additives can be used alone or in combination of two or more.
The total content of these other additives may be appropriately determined as desired, and is not particularly limited. However, in consideration of the effect of adding the other additives, 0.1 to 20 mass based on the total amount of the composition. % Is preferable, 1 to 15% by mass is more preferable, and 5 to 13% by mass is still more preferable.
粘度指数向上剤としては、例えば、質量平均分子量(Mw)が好ましくは500〜1,000,000、より好ましくは5,000〜800,000の非分散型ポリメタクリレート、分散型ポリメタクリレート等のポリメタクリレート;質量平均分子量(Mw)が好ましくは800〜300,000、好ましくは10,000〜200,000のオレフィン系共重合体(例えば、エチレン−プロピレン共重合体等)、分散型オレフィン系共重合体、スチレン系共重合体(例えば、スチレン−ジエン共重合体、スチレン−イソプレン共重合体等)等の重合体;などが挙げられる。 As the viscosity index improver, for example, a polydisperse such as non-dispersed polymethacrylate or dispersed polymethacrylate having a mass average molecular weight (Mw) of preferably 500 to 1,000,000, more preferably 5,000 to 800,000. Methacrylate; Olefin copolymer having a mass average molecular weight (Mw) of preferably 800 to 300,000, preferably 10,000 to 200,000 (for example, ethylene-propylene copolymer), dispersed olefin copolymer And polymers such as styrene-based copolymers (for example, styrene-diene copolymers, styrene-isoprene copolymers);
分散剤としては、例えば、ホウ素非含有コハク酸イミド類、ホウ素含有コハク酸イミド類、ベンジルアミン類、ホウ素含有ベンジルアミン類、コハク酸エステル類、脂肪酸あるいはコハク酸で代表される一価又は二価カルボン酸アミド類等の無灰系分散剤が挙げられる。 Examples of the dispersant include monovalent or divalent compounds represented by boron-free succinimides, boron-containing succinimides, benzylamines, boron-containing benzylamines, succinic esters, fatty acids or succinic acid. Examples include ashless dispersants such as carboxylic acid amides.
酸化防止剤としては、例えば、ジフェニルアミン系酸化防止剤、ナフチルアミン系酸化防止剤等のアミン系酸化防止剤;モノフェノール系酸化防止剤、ジフェノール系酸化防止剤、ヒンダードフェノール系酸化防止剤等のフェノール系酸化防止剤;三酸化モリブデン及び/又はモリブデン酸とアミン化合物とを反応させてなるモリブデンアミン錯体等のモリブデン系酸化防止剤;などが挙げられる。 Examples of the antioxidant include amine-based antioxidants such as diphenylamine-based antioxidants and naphthylamine-based antioxidants; monophenol-based antioxidants, diphenol-based antioxidants, hindered phenol-based antioxidants, etc. Phenolic antioxidants; molybdenum trioxides and / or molybdenum antioxidants such as molybdenum amine complexes formed by reacting molybdic acid with amine compounds; and the like.
極圧剤としては、硫化油脂、硫化脂肪酸、硫化エステル、硫化オレフィン、ジヒドロカルビルポリサルファイド、チアジアゾール化合物、アルキルチオカルバモイル化合物、チオカーバメート化合物等の硫黄系極圧剤;リン酸エステル、亜リン酸エステル、酸性リン酸エステル、酸性亜リン酸エステル及びこれらのアミン塩等のリン系極圧剤;ジアルキルチオカルバミン酸亜鉛(Zn−DTC)、ジアルキルチオカルバミン酸モリブデン(Mo−DTC)、ジアルキルジチオリン酸亜鉛(Zn−DTP)、ジアルキルジチオリン酸モリブデン(Mo−DTP)等の硫黄−リン系極圧剤;などが挙げられる。 Extreme pressure agents include sulfurized fats and oils, sulfurized fatty acids, sulfurized esters, sulfurized olefins, dihydrocarbyl polysulfides, thiadiazole compounds, alkylthiocarbamoyl compounds, thiocarbamate compounds, etc .; phosphate esters, phosphites, acidic Phosphorus-based extreme pressure agents such as phosphate esters, acidic phosphites and their amine salts; zinc dialkylthiocarbamate (Zn-DTC), molybdenum dialkylthiocarbamate (Mo-DTC), zinc dialkyldithiophosphate (Zn) -DTP) and sulfur-phosphorus extreme pressure agents such as molybdenum dialkyldithiophosphate (Mo-DTP).
また、金属不活性化剤としては、ベンゾトリアゾール系、トリルトリアゾール系、チアジアゾール系、及びイミダゾール系化合物等が挙げられ、消泡剤としては、シリコーン油、フルオロシリコーン油及びフルオロアルキルエーテル等が挙げられる。 Examples of the metal deactivator include benzotriazole, tolyltriazole, thiadiazole, and imidazole compounds, and examples of the antifoaming agent include silicone oil, fluorosilicone oil, and fluoroalkyl ether. .
(潤滑油組成物の各種物性)
本実施形態の潤滑油組成物の40℃における動粘度は、好ましくは3mm2/s以上50mm2/s以下、より好ましくは5mm2/s以上30mm2/s以下、更に好ましくは10mm2/s以上20mm2/s以下である。本実施形態の潤滑油組成物の100℃における動粘度は、好ましくは0.5mm2/s以上15mm2/s以下、より好ましくは1mm2/s以上10mm2/s以下、更に好ましくは1.5mm2/s以上5mm2/s以下である。また、本実施形態の潤滑油組成物の粘度指数は、好ましくは75以上、より好ましくは80以上、更に好ましくは85以上である。
なお、本明細書において、動粘度、及び粘度指数は、JIS K2283:2000に準じ、ガラス製毛管式粘度計を用いて測定した値である。
(Various physical properties of lubricating oil composition)
Kinematic viscosity at 40 ° C. of the lubricating oil composition of the present embodiment is preferably 3 mm 2 / s or more 50 mm 2 / s or less, more preferably 5 mm 2 / s or more 30 mm 2 / s or less, more preferably 10 mm 2 / s This is 20 mm 2 / s or less. The kinematic viscosity at 100 ° C. of the lubricating oil composition of the present embodiment is preferably 0.5 mm 2 / s to 15 mm 2 / s, more preferably 1 mm 2 / s to 10 mm 2 / s, and still more preferably 1. is less than or equal to 5mm 2 / s or more 5mm 2 / s. Further, the viscosity index of the lubricating oil composition of the present embodiment is preferably 75 or more, more preferably 80 or more, and still more preferably 85 or more.
In the present specification, the kinematic viscosity and the viscosity index are values measured using a glass capillary viscometer according to JIS K2283: 2000.
本実施形態の潤滑油組成物の−40℃のブルックフィールド粘度(BF粘度)は、好ましくは15,000mPa・s以下、より好ましくは14,900mPa・s以下、更に好ましくは14,800mPa・s以下、特に好ましくは14,750mPa・s以下である。このように、本実施形態の潤滑油組成物は、−40℃のブルックフィールド粘度(BF粘度)が小さく、優れた低温流動性を有するものである。
なお、本明細書において、−40℃のブルックフィールド粘度(BF粘度)は、ASTM D2983−09に準拠して測定したものである。
The Brookfield viscosity (BF viscosity) at −40 ° C. of the lubricating oil composition of the present embodiment is preferably 15,000 mPa · s or less, more preferably 14,900 mPa · s or less, and further preferably 14,800 mPa · s or less. Particularly preferably, it is 14,750 mPa · s or less. Thus, the lubricating oil composition of this embodiment has a low Brookfield viscosity (BF viscosity) of −40 ° C. and excellent low temperature fluidity.
In this specification, the Brookfield viscosity (BF viscosity) at −40 ° C. is measured in accordance with ASTM D2983-09.
本実施形態の潤滑油組成物のJIS K2265−4:2007に準拠し、クリーブランド開放法により測定される引火点は、好ましくは140℃以上、より好ましくは145℃以上、更に好ましくは150℃以上であり、特に好ましくは155℃以上である。このように、本実施形態の潤滑油組成物は、引火点が高く、難燃性が高く、安全性が高いものである。 In accordance with JIS K2265-4: 2007 of the lubricating oil composition of the present embodiment, the flash point measured by the Cleveland open method is preferably 140 ° C. or higher, more preferably 145 ° C. or higher, still more preferably 150 ° C. or higher. Yes, particularly preferably 155 ° C. or higher. Thus, the lubricating oil composition of the present embodiment has a high flash point, high flame retardancy, and high safety.
また、本実施形態の潤滑油組成物の120℃におけるトラクション係数は、好ましくは0.050以上、より好ましくは0.053以上、更に好ましくは0.055以上である。このように、本実施形態の潤滑油組成物は、120℃におけるトラクション係数は高いものであり、高トラクション係数と優れた低温流動性とをより高い次元で両立するとともに、高引火点を有する潤滑油組成物である。
なお、本明細書において、120℃におけるトラクション係数は、トラクション係数計測器(製品名:MTM2(Mini Traction Machine2、PCS Instruments社製)を用いて測定した値である。ここで、120℃におけるトラクション係数の測定条件は以下の通りである。まず、油タンクをヒーターで加熱することにより、油温を140℃とし、荷重70N、平均転がり速度3.8m/s、すべり率5%におけるトラクション係数を測定した。
Further, the traction coefficient at 120 ° C. of the lubricating oil composition of the present embodiment is preferably 0.050 or more, more preferably 0.053 or more, and still more preferably 0.055 or more. As described above, the lubricating oil composition of the present embodiment has a high traction coefficient at 120 ° C., and has a high traction coefficient and excellent low-temperature fluidity at a higher level, and has a high flash point. It is an oil composition.
In this specification, the traction coefficient at 120 ° C. is a value measured using a traction coefficient measuring device (product name: MTM2 (Mini Traction Machine 2, manufactured by PCS Instruments), where traction coefficient at 120 ° C. The measurement conditions are as follows: First, by heating the oil tank with a heater, the oil temperature is 140 ° C., the load is 70 N, the average rolling speed is 3.8 m / s, and the traction coefficient is measured at a slip rate of 5%. did.
(潤滑油組成物の用途)
本実施形態の潤滑油組成物は、無段変速機、無段増速機及び無段減速機、中でも無段変速機用途に好適に用いることができる。無段変速機には金属ベルト方式、チェーン方式及びトラクションドライブ方式等があるが、いずれの方式でも高い伝達効率が求められ、トラクション係数の高い潤滑油が求められる。この点で、本実施形態の潤滑油組成物はいずれもの方式の無段変速機に好適に用いることができ、とりわけトラクションドライブ方式の変速機に好適に用いることができる。
また、本実施形態の潤滑油組成物は、トラクション係数、特に高温におけるトラクション係数と低温流動性とに優れるため、例えば、自動車及び航空エンジン発電機における無段変速機用、特にトラクションドライブ方式の変速機用流体として好適に用いることができる。上記の他、建設機械及び農業機械の駆動部、風力発電の増速器等の産業用途における無段変速機、並びに無段増速機及び無段減速機にも好適に用いることができる。
(Use of lubricating oil composition)
The lubricating oil composition of the present embodiment can be suitably used for continuously variable transmissions, continuously variable speed increasers and continuously variable speed reducers, especially for continuously variable transmission applications. The continuously variable transmission includes a metal belt method, a chain method, a traction drive method, and the like, but any method requires high transmission efficiency and requires a lubricating oil having a high traction coefficient. In this respect, the lubricating oil composition of the present embodiment can be suitably used for any type of continuously variable transmission, and can be particularly suitably used for a traction drive type transmission.
Further, since the lubricating oil composition of the present embodiment is excellent in traction coefficient, particularly traction coefficient at high temperature and low-temperature fluidity, for example, for continuously variable transmissions in automobiles and aircraft engine generators, especially traction drive type gear shifting. It can be suitably used as a machine fluid. In addition to the above, it can also be suitably used for continuously variable transmissions in industrial applications, such as drive units for construction machines and agricultural machines, speed increasers for wind power generation, and continuously variable speed increasers and continuously variable speed reducers.
[潤滑油組成物の製造方法]
本実施形態の潤滑油組成物の製造方法は、引火点が140℃以上のナフテン系合成油(a)と、分岐鎖を有する炭素数5〜32のエステル(b)とを、該ナフテン系合成油(a)の組成物全量基準の含有量が35質量%以上80質量%未満となるように配合することを特徴とするものである。
[Method for producing lubricating oil composition]
The manufacturing method of the lubricating oil composition of the present embodiment comprises a naphthenic synthetic oil (a) having a flash point of 140 ° C. or higher and an ester (b) having 5 to 32 carbon atoms having a branched chain. It mix | blends so that content of the composition whole quantity reference | standard of oil (a) may be 35 to less than 80 mass%.
本実施形態の潤滑油組成物の製造方法において、引火点が140℃以上のナフテン系合成油(a)、及び分岐鎖を有する炭素数5〜32のエステル(b)は、本実施形態の潤滑油組成物に含まれる各々ナフテン系合成油(a)、及びエステル(b)として説明したものと同じであり、これらナフテン系合成油(a)、及びエステル(b)の含有量も、本実施形態の潤滑油組成物の含有量として説明したものと同じである。また、本実施形態の潤滑油組成物の製造方法において、ナフテン系合成油(a)、エステル(b)以外の成分、例えば本実施形態の潤滑油組成物に含み得る成分として説明したその他添加剤を配合してもよい。 In the method for producing a lubricating oil composition of the present embodiment, the naphthenic synthetic oil (a) having a flash point of 140 ° C. or higher and the ester having a branched chain having 5 to 32 carbon atoms (b) are the lubricants of the present embodiment. Each of the naphthenic synthetic oil (a) and ester (b) contained in the oil composition is the same as that described for the naphthenic synthetic oil (a) and ester (b). It is the same as what was demonstrated as content of the lubricating oil composition of a form. Further, in the method for producing the lubricating oil composition of the present embodiment, other additives described as components other than the naphthenic synthetic oil (a) and the ester (b), for example, components that can be included in the lubricating oil composition of the present embodiment. May be blended.
潤滑油組成物を製造するに際し、ナフテン系合成油(a)とエステル(b)との配合において、配合する順序は特に制限はなく、ナフテン系合成油(a)にエステル(b)を加えてもよいし、エステル(b)にナフテン系合成油(a)を加えてもよい。また、その他添加剤を配合する場合、その他添加剤として用いる各種添加剤を、ナフテン系合成油(a)、エステル(b)、又はナフテン系合成油(a)とエステル(b)とを配合したものに、逐次配合してもよいし、該各種添加剤を予め配合してから、配合してもよい。 When producing the lubricating oil composition, the blending order of the naphthenic synthetic oil (a) and the ester (b) is not particularly limited, and the ester (b) is added to the naphthenic synthetic oil (a). Alternatively, naphthenic synthetic oil (a) may be added to ester (b). Moreover, when mix | blending other additives, the various additives used as other additives mix | blended naphthenic synthetic oil (a), ester (b), or naphthenic synthetic oil (a) and ester (b). The ingredients may be blended sequentially, or the various additives may be blended in advance.
[無段変速機]
本実施形態の無段変速機は、引火点が140℃以上のナフテン系合成油(a)及び分岐鎖を有する炭素数5〜32のエステル(b)を含み、該ナフテン系合成油(a)の組成物全量基準の含有量が35質量%以上80質量%未満である潤滑油組成物が用いられることを特徴とするものである。
本実施形態の無段変速機に用いられる潤滑油組成物は、本実施形態の潤滑油組成物として説明したものと同じである。
[Continuously variable transmission]
The continuously variable transmission of the present embodiment includes a naphthenic synthetic oil (a) having a flash point of 140 ° C. or higher and an ester (b) having 5 to 32 carbon atoms having a branched chain, and the naphthenic synthetic oil (a). A lubricating oil composition having a content based on the total amount of the composition of 35% by mass or more and less than 80% by mass is used.
The lubricating oil composition used in the continuously variable transmission of the present embodiment is the same as that described as the lubricating oil composition of the present embodiment.
無段変速機としては、金属ベルト方式、チェーン方式及びトラクションドライブ方式等があるが、いずれの方式の無段変速機でもよく、用いられる潤滑油組成物が高トラクション係数と優れた低温流動性とをより高い次元で両立するとともに、高引火点を有するという特徴を有しており、この特徴をより有効に活用する観点から、好ましくはトラクションドライブ方式の無段変速機である。 As the continuously variable transmission, there are a metal belt method, a chain method, a traction drive method, etc., any type of continuously variable transmission may be used, and the lubricating oil composition used has a high traction coefficient and excellent low temperature fluidity. In addition, the traction drive type continuously variable transmission is preferable from the viewpoint of more effectively utilizing this feature.
次に、実施例により本発明をさらに具体的に説明するが、本発明はこれらの例によって何ら制限されるものではない。 EXAMPLES Next, although an Example demonstrates this invention further more concretely, this invention is not restrict | limited at all by these examples.
潤滑油組成物の性状及び性能の測定は以下の方法で行った。
(1)動粘度
JIS K 2283:2000に準拠し、40℃、100℃における動粘度を測定した。
(2)粘度指数(VI)
JIS K 2283:2000に準拠して測定した。
(3)120℃におけるトラクション係数
トラクション係数計測器(製品名:MTM2(Mini Traction Machine2、PCS Instruments社製)を用い、下記測定条件において測定した値である。0.050以上であれば合格である。
油温の加熱条件:140℃
荷重:70N
平均転がり速度:3.8m/s
すべり率:5%
(4)−40℃におけるブルックフィールド粘度
−40℃のブルックフィールド粘度(BF粘度)は、ASTM D2983−09に準拠して測定した。15,000mPa・s以下であれば合格である。
(5)引火点
JIS K2265−4:2007(引火点の求め方−第4部:クリーブランド開放法)に準拠し、クリーブランド開放法により測定した。140℃以上であれば合格である。
The properties and performance of the lubricating oil composition were measured by the following method.
(1) Kinematic viscosity Based on JISK2283: 2000, the kinematic viscosity in 40 degreeC and 100 degreeC was measured.
(2) Viscosity index (VI)
It measured based on JISK2283: 2000.
(3) Traction coefficient at 120 ° C. A traction coefficient measuring instrument (product name: MTM2 (Mini Traction Machine 2, manufactured by PCS Instruments)) is a value measured under the following measurement conditions. .
Oil temperature heating condition: 140 ° C
Load: 70N
Average rolling speed: 3.8 m / s
Slip rate: 5%
(4) Brookfield viscosity at −40 ° C. The Brookfield viscosity (BF viscosity) at −40 ° C. was measured according to ASTM D2983-09. If it is 15,000 mPa · s or less, it is acceptable.
(5) Flash point Measured by the Cleveland open method according to JIS K2265-4: 2007 (How to determine the flash point-Part 4: Cleveland open method). If it is 140 degreeC or more, it is a pass.
(実施例1〜5、比較例1〜5の潤滑油組成物の作製)
下記表1に示す配合処方に従い配合して、潤滑油組成物を作製した。得られた各潤滑油組成物について、上記方法により測定した各性状及び性能の評価結果を表1に示す。
(Production of lubricating oil compositions of Examples 1 to 5 and Comparative Examples 1 to 5)
A lubricating oil composition was prepared by blending according to the blending formulation shown in Table 1 below. Table 1 shows the evaluation results of the properties and performances measured by the above methods for the obtained lubricating oil compositions.
本実施例で用いた表1に記載のナフテン系合成油、エステル1〜4、及びロンギホレンは以下化学式で示されるものである。 The naphthenic synthetic oils, esters 1 to 4, and longifolene shown in Table 1 used in this example are represented by the following chemical formulas.
・ナフテン系合成油:一般式(1)において、R11及びR13がメチル基であり、R12がメチレン基であり、X11及びX12がビシクロ[2.2.1]ヘプタン環であり、p11が2、p12が1である合成油である。
・エステル1:一般式(2)において、R21が3,5,5−トリメチルヘキシル基であり、R22が2,4,4−トリメチルペンチル基であるモノエステルである。
・エステル2:一般式(3)において、R31及びR32がイソプロピル基であり、X31が2,2,4−トリメチルペンチル−1,3−ジイル基であるジエステルである。
・エステル3:一般式(3)において、R31及びR32が2,4,4−トリメチルペンチル基であり、X31が3−メチルペンチル−1,5−ジイル基であるジエステルである。
・エステル4:一般式(3)において、R31及びR32が2,4,4−トリメチルペンチル基であり、X31が2,2−ジメチルプロピル−1,3−ジイル基であるジエステルである。
・添加剤:粘度指数向上剤(実施例1〜4、比較例1〜5において組成物全量基準の含有量として1.5質量%含む。)、その他、分散剤(コハク酸イミド)、酸化防止剤、極圧剤、金属不活性化剤、及び消泡剤
-Naphthenic synthetic oil: In the general formula (1), R 11 and R 13 are methyl groups, R 12 is a methylene group, and X 11 and X 12 are bicyclo [2.2.1] heptane rings , P 11 is 2 and p 12 is 1.
Ester 1: A monoester in which R 21 is a 3,5,5-trimethylhexyl group and R 22 is a 2,4,4-trimethylpentyl group in the general formula (2).
Ester 2: In general formula (3), R 31 and R 32 are isopropyl groups, and X 31 is a 2,2,4-trimethylpentyl-1,3-diyl group.
Ester 3: In general formula (3), R 31 and R 32 are 2,4,4-trimethylpentyl groups and X 31 is a 3-methylpentyl-1,5-diyl group.
Ester 4: In the general formula (3), R 31 and R 32 are 2,4,4-trimethylpentyl groups, and X 31 is a 2,2-dimethylpropyl-1,3-diyl group. .
Additive: Viscosity index improver (in Examples 1 to 4 and Comparative Examples 1 to 5 containing 1.5% by mass as the content based on the total amount of the composition), other dispersant (succinimide), antioxidant Agent, extreme pressure agent, metal deactivator, and antifoaming agent
表1の結果から、本実施形態の潤滑油組成物は、いずれもトラクション係数が0.050以上であり、−40℃でのブルックフィールド粘度が15,000mPa・s以下であり、また引火点が140℃以上であることから、高トラクション係数と優れた低温流動性とをより高い次元で両立するとともに、高引火点を有するものであることが確認された。
一方、ナフテン系合成油(a)の含有量が35質量%未満であり、かつエステル(b)を含まない比較例1の潤滑油組成物は引火点が120℃と低いものであり、ナフテン系合成油(a)の含有量が80質量%以上である比較例2の潤滑油組成物は−40℃でのブルックフィールド粘度が60,000mPa・s以上と極めて大きく低温流動性に劣るものであることが確認された。また、ナフテン系合成油(a)を含まない比較例3〜5の潤滑油組成物はいずれもトラクション係数が0.050未満と低く、高トラクション係数を有するものとはいえないものであった。
From the results in Table 1, the lubricating oil composition of this embodiment has a traction coefficient of 0.050 or more, a Brookfield viscosity at −40 ° C. of 15,000 mPa · s or less, and a flash point. Since it is 140 degreeC or more, while confirming that a high traction coefficient and the outstanding low-temperature fluidity were compatible in a higher dimension, it was confirmed that it has a high flash point.
On the other hand, the lubricating oil composition of Comparative Example 1 in which the content of the naphthenic synthetic oil (a) is less than 35% by mass and does not contain the ester (b) has a low flash point of 120 ° C. The lubricating oil composition of Comparative Example 2 in which the content of the synthetic oil (a) is 80% by mass or more has a very large Brookfield viscosity at −40 ° C. of 60,000 mPa · s or more and is inferior in low-temperature fluidity. It was confirmed. In addition, the lubricating oil compositions of Comparative Examples 3 to 5 containing no naphthenic synthetic oil (a) had a traction coefficient as low as less than 0.050 and could not be said to have a high traction coefficient.
Claims (15)
(一般式(1)中、R11及びR13はそれぞれ独立に1価の炭化水素基を示し、R12は2価の炭化水素基を示し、X11及びX12はそれぞれ独立にシクロへキサン環、ビシクロヘプタン環又はビシクロオクタン環を示し、p11及びp12はそれぞれ独立に1以上6以下の整数を示す。) The lubricating oil composition according to claim 1, wherein the naphthenic synthetic oil (a) is a synthetic oil represented by the following general formula (1).
(In the general formula (1), R 11 and R 13 each independently represent a monovalent hydrocarbon group, R 12 represents a divalent hydrocarbon group, and X 11 and X 12 each independently represent cyclohexane. A ring, a bicycloheptane ring or a bicyclooctane ring, and p 11 and p 12 each independently represents an integer of 1 to 6.
(一般式(2)中、R21及びR22は、それぞれ独立に炭素数3以上の分岐状の1価の炭化水素基を示す。また、一般式(3)中、R31及びR32は、それぞれ独立に炭素数3以上の分岐状の1価の炭化水素基を示し、X31は炭素数3以上の分岐状の2価の炭化水素基を示す。) The ester (b) is at least one ester selected from a monoester represented by the following general formula (2) and a diester represented by the following general formula (3). The lubricating oil composition described in 1.
(In General Formula (2), R 21 and R 22 each independently represent a branched monovalent hydrocarbon group having 3 or more carbon atoms. In General Formula (3), R 31 and R 32 are And each independently represents a branched monovalent hydrocarbon group having 3 or more carbon atoms, and X 31 represents a branched divalent hydrocarbon group having 3 or more carbon atoms.)
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CN201980003763.2A CN111032835B (en) | 2018-01-29 | 2019-01-28 | Lubricating oil composition, method for producing lubricating oil composition, and continuously variable transmission |
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US10927321B2 (en) | 2019-03-13 | 2021-02-23 | Valvoline Licensing And Intellectual Property Llc | Traction fluid with improved low temperature properties |
CN114901790A (en) * | 2019-10-30 | 2022-08-12 | 胜牌许可和知识产权有限公司 | Traction fluid with improved low temperature characteristics |
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JP7016733B2 (en) * | 2018-03-13 | 2022-02-07 | 出光興産株式会社 | Lubricating oil composition, manufacturing method of lubricating oil composition and continuously variable transmission |
FR3093729A1 (en) | 2019-03-13 | 2020-09-18 | Total Marketing Services | Use of an ester in a cooling composition |
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